6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150
FDA 510(k)
FDA Unclassified
·Unknown
COMPLEMENT C4 FOR THE TECHNICON DPA-1(TM) SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver
FDA 510(k)
FDA Class 2
·Orthopedic
MP50 INTELLIVUE PATIENT MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MHX·June 16, 2014
SMART CONTROL NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIO·February 28, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 13, 2011